{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Mentor",
      "address_1": "5976 Heisley Rd",
      "reason_for_recall": "Packaging non-conformance related to the integrity of the sterile pouch seal.",
      "address_2": "",
      "product_quantity": "100 units",
      "code_info": "Lot 1417696",
      "center_classification_date": "20141223",
      "distribution_pattern": "Distributed to the states of FL, MO, OH and WI.",
      "state": "OH",
      "product_description": "UroSeal Adjustable Endoscopic Valve.  Model/Catalog # 00913410  The primary packaging is a Tyvek pouch.  The secondary package is a corrugate box.  5 units per box.    Used to cover the opening to the biopsy/suction channel of an endoscope.",
      "report_date": "20141231",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "US Endoscopy Group Inc",
      "recall_number": "Z-0861-2015",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "69809",
      "termination_date": "20150601",
      "more_code_info": "",
      "recall_initiation_date": "20141031",
      "postal_code": "44060-1873",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}